A novel mutation (C271F) in the Notch3 gene in a Chinese man with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Clinica Chimica Acta

Volumn 376, Issue 1-2, 2007, Pages 229-232

  Au, Kam Ming ^a   Li, Ho Lun ^a   Sheng, Bun ^a   Chow, Tat Chong ^a   Chen, Mo Lung ^a   Lee, Kam Cheong ^a   Chan, Albert Yan Wo ^a  

^a PRINCESS MARGARET HOSPITAL   (Hong Kong)

Author keywords

CADASIL; Notch3; Stroke

Indexed keywords

NOTCH3 RECEPTOR;

ADULT; ALLELE; ARTERY DISEASE; ARTICLE; CASE REPORT; DNA SEQUENCE; ELECTRON MICROSCOPY; GENE AMPLIFICATION; GENE IDENTIFICATION; GENE MUTATION; HETEROZYGOSITY; HUMAN; LEUKOENCEPHALOPATHY; MALE; PRIORITY JOURNAL;

ASIAN CONTINENTAL ANCESTRY GROUP; CADASIL; CAPILLARIES; DNA MUTATIONAL ANALYSIS; GENES, DOMINANT; HUMANS; MALE; MIDDLE AGED; MUTATION; PEDIGREE; RECEPTORS, NOTCH;

EID: 33845332739     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cca.2006.07.022     Document Type: Article

References (13)

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